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羌活(Notopterygium incisum)nrDNAITS和cpDNA rpl20-rps1序列分子进化特点的分析 被引量:1
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作者 杨路存 刘何春 +2 位作者 周学丽 徐文华 周国英 《植物研究》 CAS CSCD 北大核心 2016年第2期291-296,共6页
应用PCR产物直接测序法分析了羌活居群间nrDNA(核糖体DNA)ITS序列和cpDNA(叶绿体DNA)rpl20-rps12的碱基差异,从而初步研究两套植物基因组的变异速率。采用改良的CTAB法从硅胶干燥的羌活叶片中提取总DNA,并对nrDNA ITS和cpDNA rpl20-rps1... 应用PCR产物直接测序法分析了羌活居群间nrDNA(核糖体DNA)ITS序列和cpDNA(叶绿体DNA)rpl20-rps12的碱基差异,从而初步研究两套植物基因组的变异速率。采用改良的CTAB法从硅胶干燥的羌活叶片中提取总DNA,并对nrDNA ITS和cpDNA rpl20-rps12区域进行扩增、纯化、测序。nrDNAITS序列共有635 bp,有变异位点17处,变异位点百分率为2.68%,(G+C)含量为57.83%。cpDNA rpl20-rps12序列共有767 bp,有变异位点35处,变异位点百分率4.56%,(G+C)含量为33.06%。比较发现,羌活nrDNAITS区域较cpDNA rpl20-rps12序列保守,变异速率较慢。通过对ITS和rpl20-rps12序列单倍型(haplotype)进行分析发现,两者得出的结论一致,即现有分布范围经历了居群近期范围扩张。因此,羌活nrDNA ITS序列适合该种的谱系地理学研究。 展开更多
关键词 羌活 ITS序列 rpl20-rps12序列
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窄叶鲜卑花(Sibiraea angustata)nrDNA ITS和cpDNA trnL-F序列分子进化特点的分析 被引量:10
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作者 段义忠 张得钧 +3 位作者 高庆波 张发起 李印虎 陈世龙 《植物研究》 CAS CSCD 北大核心 2010年第2期146-151,共6页
应用PCR产物直接测序法分析了窄叶鲜卑花居群间nrDNA(核糖体DNA)ITS序列和cpDNA(叶绿体DNA)trnL-F的碱基差异,并与cpDNAtrnS-G序列和rpl20-rps12序列进行比较,从而初步研究两套植物基因组的变异速率。采用改良的CTAB法从硅胶干燥的窄叶... 应用PCR产物直接测序法分析了窄叶鲜卑花居群间nrDNA(核糖体DNA)ITS序列和cpDNA(叶绿体DNA)trnL-F的碱基差异,并与cpDNAtrnS-G序列和rpl20-rps12序列进行比较,从而初步研究两套植物基因组的变异速率。采用改良的CTAB法从硅胶干燥的窄叶鲜卑花叶片中提取总DNA,并对nrDNA ITS和cpDNAtrnL-F区域进行扩增、纯化、测序。nrDNA ITS序列共有601 bp,有变异位点3处,变异位点百分率为0.05%,(G+C)含量为41.4%。cpDNAtrnL-F序列共有927 bp,有变异位点1处,变异位点百分率0.01%,(G+C)含量为32.6%,两种序列的核苷酸多样性非常低。比较发现,窄叶鲜卑花nrDNA ITS区域较cpDNAtrnS-G序列和rpl20-rps12序列保守,变异速率较慢,比cpDNAtrnL-F序列变异速率稍快。通过对ITS序列单倍型(haplotype)进行分析发现,窄叶鲜卑花现有分布范围经历了居群近期范围扩张,与叶绿体基因组(trnS-G和rpl20-rps12序列)得出的结论一致。因此,窄叶鲜卑花nrDNA ITS序列适合该种的谱系地理学研究。 展开更多
关键词 窄叶鲜卑花 ITS序列 TRNL-F序列 trnS-G序列 rpl20-rps12序列
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西川红景天nrDNA ITS序列初步研究 被引量:1
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作者 高庆波 张得钧 +2 位作者 段义忠 张发起 陈世龙 《安徽农业科学》 CAS 北大核心 2009年第1期49-50,89,共3页
[目的]对西川红景天nrDNA ITS序列进行分析,并与cpDNA(叶绿体DNA)trnS-trnG序列和rpl20-rps12序列进行比较,从而初步比较2套植物基因组的进化速率。[方法]采用改良CTAB法从硅胶干燥的西川红景天叶片中提取总DNA,并对nrDNA ITS区进行扩... [目的]对西川红景天nrDNA ITS序列进行分析,并与cpDNA(叶绿体DNA)trnS-trnG序列和rpl20-rps12序列进行比较,从而初步比较2套植物基因组的进化速率。[方法]采用改良CTAB法从硅胶干燥的西川红景天叶片中提取总DNA,并对nrDNA ITS区进行扩增、纯化、测序,然后与cpDNAtrnS-trnG和rpl20-rps12序列进行比较。[结果]序列比对后得到长度为701 bp的ITS序列,其中变异位点13处,占总序列的1.85%。在13处变异位点中,8处为碱基置换,5处为插入/缺失。(A+T)含量为46.9%,(G+C)含量为53.1%。核苷酸多样性为0.004 27。[结论]西川红景天nrDNA ITS区域较cpDNAtrnS-trnG序列和rpl20-rps12序列保守,进化速率较慢。 展开更多
关键词 西川红景天 ITS序列 trnS-trnG序列 rpl20-rps12序列
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Phylogenetic Relationship of an Extremely Endangered Species, Pinus squamata (Pinaceae) Inferred from Four Sequences of the Chloroplast Genome and ITS of the Nuclear Ribosomal DNA 被引量:1
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作者 张志勇 杨俊波 李德铢 《Acta Botanica Sinica》 CSCD 2003年第5期530-535,共6页
Pinus squamata X. W. Li, a recently-described species of the Pinaceae, is an extremely endangered pine with only 32 individuals in the wild. This species was thought to be intermediate between P. bungeana Zuec. ex End... Pinus squamata X. W. Li, a recently-described species of the Pinaceae, is an extremely endangered pine with only 32 individuals in the wild. This species was thought to be intermediate between P. bungeana Zuec. ex Endl. of subgen. Strobus and P. yunnanensis Franch. of subgen. Pinus by the original author. We made an effort to address the question of the phylogenetic relationship of this peculiar and important species in the context of the major groups of the genus Pinus by using sequences of the rbcL, matK,genes, rpl20-rps18 spacer, trnV intron of the chloroplast genome and the nuclear ribosomal ITS region. The results of the separated analysis and the combined analysis of the four cpDNA sequences and ITS sequence indicated that P. squamata was a stable member of subsect. Gerardianae and P. gerardiana Wall. was the closest species of P. squamata phylogenetically. As a result, the causes of the distribution pattern of subsect. Gerardianae were also discussed. 展开更多
关键词 Pinus squamata phylogenetic relationship rbc L mat K rpl20-rps 18 trn V ITS
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Preliminary Study on the ITS Sequences of nrDNA from Rhodiola alsia
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作者 高庆波 张得钧 +2 位作者 段义忠 张发起 陈世龙 《Agricultural Science & Technology》 CAS 2008年第5期63-65,149,共4页
[Objective] The study aimed to analyze the ITS sequences of nrDNA from Rhodiola alisa and investigate the difference of evolution rate between nrDNA and trnS-trnG and rpl20-rps12 sequences of cpDNA(chloroplast DNA).[M... [Objective] The study aimed to analyze the ITS sequences of nrDNA from Rhodiola alisa and investigate the difference of evolution rate between nrDNA and trnS-trnG and rpl20-rps12 sequences of cpDNA(chloroplast DNA).[Method]Total DNA was extracted from silica-dried leaves of R.alsia by using modified CTAB method.With the extracted DNA sample as template,nrDNA ITS region was amplified,then purified and sequenced.In addition,the yielded ITS sequences were also compared with the known trnS-trnG and rpl20-rps12 sequences of cpDNA from R.alsia.[Result]The ITS sequence of nrDNA from R.alsia was 701 bp in length,of which 13 variable sites were found with a percentage of 1.85%.Of the 13 variable sites,8 were caused by point mutations,5 were the results of insertions or deletions.The(A+T)content and(G+C)content were 46.9% and 53.1%,respectively.The nucleotide diversity(π)was 0.004 27.[Conclusion]The ITS region of nrDNA from R.alsia was more conservative and evolved more slowly than the trnS-trnG and rpl20-rps12 sequences of its cpDNA. 展开更多
关键词 RHODIOLA alsia ITS SEQUENCE trnS-trnG SEQUENCE rpl20-rps12 SEQUENCE
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